https://www.selleckchem.com/pr....oducts/pf-06650833.h
https://www.selleckchem.com/pr....oducts/pf-06650833.h
Impaired colour separation regarding HE discolored histological photographs simply by linearly modifying the color place. BACKGROUND Point and copy number variant mutations in the PRRT2 gene have been identified in a variety of paroxysmal disorders and different types of epilepsy. In this study, we analyzed the phenotypes and PRRT2-related mutations in Chinese epilepsy children. METHODS A total of 492 children with epilepsy were analyzed by whole exome sequencing (WES)
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